Towards biologically inspired materials

G. Babini, A. Tampieri
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引用次数: 11

Abstract

Abstract The development of a synthetic bone substitute able to mimic both the chemical composition and morphology of bone's inorganic component is a priority for biomaterials research. Hydroxyapatite is a promising material for this application. The role of nanostructured apatites in the design and preparation of biomimetic and bioactive scaffolds is particularly crucial. These new materials chacterised by nanodomain and modified chemical features show improved performance in terms of interaction with natural tissue, allowing and taking part in bone ingrowth. Thus interest has shifted from biocompatible to biomimetic and bioactive materials. The importance of non-stoichiometric/defective apatites similar to the mineral part of bone, in particular those containing HPO42- CO32- and Mg2+, is explained. Attention is focused on innovative synthesis techniques that can yield powders with higher reactivity to build synthetic implants with a porous structure resembling that of spongy bone that can ensure complete penetration and consequent replacement of the bony tissue. The use of cellulosic sponges soaked with powder suspensions can give adequate porosity in terms of both size and distribution, and this appears to be a suitable method for the repair of both loadbearing and nonloadbearing osseous defects. Such sponges can also function as in situ drug delivery systems if they are charged with pharmacologically active compounds. So far the characteristics of artificial bone tissues have been shown to be very different from those of natural bone, mainly because of the absence of the self-organising interaction between apatites and the proteinic component that modifies the intrinsic features of each constituent. For that reason attention is currently focused on so called biologically inspired materials, in this case composites synthesised to exploit the ability of biological systems to store and process information at the molecular level. Following this new approach, nanosize bladelike crystals of hydroxyapatite have been nucleated in situ on self-assembling collagen fibres. The characteristics of the resulting composites are described.
走向生物启发材料
开发一种能够模拟骨无机成分的化学成分和形态的合成骨替代品是生物材料研究的重点。羟基磷灰石是一种很有前途的材料。纳米结构磷灰石在仿生和生物活性支架的设计和制备中的作用尤为重要。这些新材料具有纳米结构域和修饰的化学特征,在与自然组织的相互作用方面表现出更好的性能,允许并参与骨长入。因此,人们的兴趣已经从生物相容性转移到仿生和生物活性材料。解释了非化学计量/缺陷磷灰石的重要性,类似于骨骼的矿物部分,特别是那些含有HPO42- CO32-和Mg2+的磷灰石。人们的注意力集中在创新的合成技术上,这些技术可以产生具有更高反应性的粉末,以构建具有类似海绵状骨的多孔结构的合成植入物,从而确保完全渗透和随后的骨组织替换。使用纤维海绵浸泡粉末悬浮液可以在大小和分布方面提供足够的孔隙度,这似乎是一种适合修复承重和非承重骨缺陷的方法。这种海绵也可以作为原位药物输送系统,如果它们被药理活性化合物充电。到目前为止,人工骨组织的特征已被证明与天然骨组织有很大的不同,主要是因为磷灰石和蛋白质成分之间缺乏自我组织的相互作用,这种相互作用可以改变每种成分的内在特征。由于这个原因,目前的注意力集中在所谓的生物启发材料上,在这种情况下,合成复合材料利用生物系统在分子水平上存储和处理信息的能力。采用这种新方法,羟基磷灰石的纳米叶片状晶体已在自组装的胶原纤维上原位成核。描述了所得复合材料的特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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